Canonical Allele Identifier: CA398639741

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208428G>A (hg19) ; chr17:g.18305114G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305114G>A , CM000679.2:g.18305114G>A	GRCh38
NC_000017.10:g.18208428G>A , CM000679.1:g.18208428G>A	GRCh37
NC_000017.9:g.18149153G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.497C>T MANE Select	ENSP00000321636.5:p.Ala166Val
ENST00000321105.9:c.497C>T	ENSP00000321636.5:p.Ala166Val
ENST00000461127.5:c.*115C>T	ENSP00000464338.1:n.*115C>T
ENST00000469739.6:n.376C>T
ENST00000542570.5:c.497C>T	ENSP00000442336.2:p.Ala166Val
ENST00000580095.5:c.422C>T	ENSP00000462790.1:p.Ala141Val
ENST00000582981.5:c.*153C>T	ENSP00000462378.1:n.*153C>T
ENST00000584582.5:c.*153C>T	ENSP00000462136.1:n.*153C>T
ENST00000584669.5:n.542+1777C>T
NM_004618.3:c.497C>T	NP_004609.1:p.Ala166Val
XM_005256776.2:c.212C>T	XP_005256833.1:p.Ala71Val
XM_011524000.1:c.497C>T	XP_011522302.1:p.Ala166Val
XM_011524001.1:c.-706C>T	XP_011522303.1:n.-706C>T
NM_001320759.1:c.212C>T	NP_001307688.1:p.Ala71Val
NM_004618.4:c.497C>T	NP_004609.1:p.Ala166Val
XM_011524001.2:c.-706C>T	XP_011522303.1:n.-706C>T
XM_024450903.1:c.-425C>T	XP_024306671.1:n.-425C>T
XR_001752601.2:n.715C>T
NM_004618.5:c.497C>T MANE Select	NP_004609.1:p.Ala166Val
NM_001320759.2:c.212C>T	NP_001307688.1:p.Ala71Val